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CHETAK NEW YORK LLC Recall: Product tested positive Salmonella .

United States

TerminatedClass I

Company
CHETAK NEW YORK LLC
Product
Deep Sprouted Mat 16 oz.
Recall date
June 28, 2025
Terminated
October 28, 2025
Source
FDA

Reason for recall

Product tested positive Salmonella .

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Deep Sprouted Mat 16 oz. Not published in this source record 5232 PACKET/BAG OF SPROUTED MAT IN24330,25072,25108,24353,25171,24297,25058,25078,24291,25107,24354 AND 24292

Distribution

  • Th recalled product was distributed to the following States: CA
  • NJ
  • IL
  • FL
  • TX

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
H-0574-2025
Event ID
97300
Status
Terminated
Classification
Class I
Company
CHETAK NEW YORK LLC
Product description
Deep Sprouted Mat 16 oz.
Quantity
5232 PACKET/BAG OF SPROUTED MAT
Reason
Product tested positive Salmonella .
Recall initiation date
June 28, 2025
Report date
September 3, 2025
Classification date
Not published in this source record
Termination date
October 28, 2025
Distribution pattern
Th recalled product was distributed to the following States: CA, NJ, IL, FL, TX
UPC, lot, and code information
IN24330,25072,25108,24353,25171,24297,25058,25078,24291,25107,24354 AND 24292
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 97300 with 1 other product entry in Public Health Trace.

FDA Recall United States Terminated Historical recordClass I

CHETAK NEW YORK LLC

Product
Deep Sprouted Moong 16 oz
Published
September 3, 2025
Distribution
Th recalled product was distributed to t…

View recall →

Responsible company: CHETAK NEW YORK LLC

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Distribution
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Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
California 1
New Jersey 1
Illinois 1
Florida 1
Texas 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.